Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 2 of 2
Full-Text Articles in Pathology
Familial Inheritance Of The 3q29 Microdeletion Syndrome: Case Report And Review, W. A. Khan, N. Cohen, S. A. Scott, E. M. Pereira
Familial Inheritance Of The 3q29 Microdeletion Syndrome: Case Report And Review, W. A. Khan, N. Cohen, S. A. Scott, E. M. Pereira
Journal Articles
No abstract provided.
Cytogenomic Identification And Long-Read Single Molecule Real-Time (Smrt) Sequencing Of A Bardet-Biedl Syndrome 9 (Bbs9) Deletion, J. Reiner, L. Pisani, W. Qiao, R. Singh, Y. Yang, L. Shi, W. A. Khan, R. Sebra, N. Cohen, S. A. Scott, +3 Additional Authors
Cytogenomic Identification And Long-Read Single Molecule Real-Time (Smrt) Sequencing Of A Bardet-Biedl Syndrome 9 (Bbs9) Deletion, J. Reiner, L. Pisani, W. Qiao, R. Singh, Y. Yang, L. Shi, W. A. Khan, R. Sebra, N. Cohen, S. A. Scott, +3 Additional Authors
Journal Articles
No abstract provided.